E. coli cells are cultured in minimal media (M9), exposed to the nematodes and lysed. A special reagent (RNAProtect, QIAGEN) is used to assure RNA is preserved during the process. It is important that the cells are harvested during their log phase, which ensures the maximum yield of information since genetic expression is at its highest.

The RNA is extracted using QIAGEN’s RNeasy Kit. Two cultures are purified in sufficient amounts to allow duplicates - one worm group and one control group. The RNA is quality checked and then stored.

Poly(A)-tails consists of adenosine nucleotides that are added onto the 3’ end of the nucleotide strand in mostly eukaryotes for translation purposes. Since these polyA tails are not present in bacteria, they need to be added onto the ends of our RNA to work as a primer target in the next step of the process.

Using our newly added Poly(A)-tails as a primer target, we subject our RNA to reverse transcription to create complementary DNA copies - or cDNA. The RNA needs to be converted into DNA to be sequenced with the MinION device. The original RNA template is then degraded and a second strand is synthesized onto the cDNA.

A necessary step to be able to make sense of the sequenced data is to attach so-called barcodes to the end of each cDNA strand. Barcodes are small sequences which are known beforehand and allows us to differentiate between different samples. Because two transcriptome samples will be sequenced at the same time, this will let us know which sequence came from which sample.

One final step before sequencing can begin is to attach the adaptor sequences onto the ends of the barcodes. These specialized adaptors allows the pores of the sequencing device to recognize the cDNA-strand and move it into the sequencing machinery.

The MinION device, produced by Oxford Nanopore Technologies, works by applying an electrical current and pulling the DNA strand through small biological pores. This movement causes changes in the electrical current also passing through the pore - and the charge of the current varies depending on which nucleotide of the DNA strand is passing through at the moment. This is what enables the sequencing - the current changes are translated into the nucleotide order of the DNA strand.

With the genetic information of the samples finally deciphered, it is time to match it to known genes in the E.coli genome and quantify the amount of genes that was expressed way back before step one of this pipeline. This allows us to see the possible difference in gene expression between the E.coli worm samples and the E.coli control samples.